Search Results - "Levinsohn, Jonathan L."

Anthrax lethal factor cleavage of Nlrp1 is required for activation of the inflammasome by Levinsohn, Jonathan L, Newman, Zachary L, Hellmich, Kristina A, Fattah, Rasem, Getz, Matthew A, Liu, Shihui, Sastalla, Inka, Leppla, Stephen H, Moayeri, Mahtab

“…NOD-like receptor (NLR) proteins (Nlrps) are cytosolic sensors responsible for detection of pathogen and danger-associated molecular patterns through unknown…”
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Anthrax lethal factor cleaves mouse nlrp1b in both toxin-sensitive and toxin-resistant macrophages by Hellmich, Kristina A, Levinsohn, Jonathan L, Fattah, Rasem, Newman, Zachary L, Maier, Nolan, Sastalla, Inka, Liu, Shihui, Leppla, Stephen H, Moayeri, Mahtab

“…Anthrax lethal factor (LF) is the protease component of anthrax lethal toxin (LT). LT induces pyroptosis in macrophages of certain inbred mouse and rat…”
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Second-Hit, Postzygotic PMVK and MVD Mutations in Linear Porokeratosis by Atzmony, Lihi, Khan, Habib M, Lim, Young H, Paller, Amy S, Levinsohn, Jonathan L, Holland, Kristen E, Mirza, Fatima Nadeem, Yin, Emily, Ko, Christine J, Leventhal, Jonathan S, Choate, Keith A

“…Linear porokeratosis features linear and whorled configurations of keratotic papules and plaques, with coronoid lamellae present on histologic examination…”
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Somatic Mutations in NEK9 Cause Nevus Comedonicus by Levinsohn, Jonathan L., Sugarman, Jeffrey L., McNiff, Jennifer M., Antaya, Richard J., Choate, Keith A.

“…Acne vulgaris (AV) affects most adolescents, and of those affected, moderate to severe disease occurs in 20%. Comedones, follicular plugs consisting of…”
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Somatic V600E BRAF Mutation in Linear and Sporadic Syringocystadenoma Papilliferum by Levinsohn, Jonathan L., Sugarman, Jeffrey L., Bilguvar, Kaya, McNiff, Jennifer M., Choate, Keith A., The Yale Center for Mendelian Genomics

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Palmoplantar Keratoderma in Costello Syndrome Responsive to Acitretin by Marukian, Nareh V., Levinsohn, Jonathan L., Craiglow, Brittany G., Milstone, Leonard M., Choate, Keith A.

“…Costello syndrome (CS) is a multisystem congenital disorder characterized by coarse facial features, cardiac defects, intellectual disability, and…”
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Identification of a gain-of-function STAT3 mutation (p.Y640F) in lymphocytic variant hypereosinophilic syndrome by Walker, Sarah, Wang, Chen, Walradt, Trent, Hong, Bok Sil, Tanner, Justin R., Levinsohn, Jonathan L., Goh, Gerald, Subtil, Antonio, Lessin, Stuart R., Heymann, Warren R., Vonderheid, Eric C., King, Brett A., Lifton, Richard P., Choi, Jaehyuk

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Somatic Mutation Profile of Atypical Fibroxanthoma and Cutaneous Undifferentiated Pleomorphic Sarcoma by Lim, Young H., Zaki, Theodore D., Levinsohn, Jonathan L., Galan, Anjela, Choate, Keith A., Hanlon, Allison M.

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A Somatic p.G45E GJB2 Mutation Causing Porokeratotic Eccrine Ostial and Dermal Duct Nevus by Levinsohn, Jonathan L, McNiff, Jennifer M, Antaya, Richard J, Choate, Keith A

“…Recent data demonstrated somatic mutations in GJB2 that were present in affected porokeratotic eccrine ostial and dermal duct nevus (PEODDN) tissue but absent…”
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Whole-Exome Sequencing Reveals Somatic Mutations in HRAS and KRAS, which Cause Nevus Sebaceus by Levinsohn, Jonathan L., Tian, Li C., Boyden, Lynn M., McNiff, Jennifer M., Narayan, Deepak, Loring, Erin S., Yun, Duri, Sugarman, Jeffrey L., Overton, John D., Mane, Shrikant M., Lifton, Richard P., Paller, Amy S., Wagner, Annette M., Antaya, Richard J., Choate, Keith A.

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Somatic HRAS p.G12S Mutation Causes Woolly Hair and Epidermal Nevi by Levinsohn, Jonathan L., Teng, Joyce, Craiglow, Brittany G., Loring, Erin C., Burrow, T Andrew, Mane, Shrikant S., Overton, John D., Lifton, Richard P., McNiff, Jennifer M., Lucky, Anne W., Choate, Keith A.

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Somatic HRAS p.G12S mutation causes woolly hair and epidermal nevi by Levinsohn, Jonathan L, Teng, Joyce, Craiglow, Brittany G, Loring, Erin C, Burrow, T Andrew, Mane, Shrikant S, Overton, John D, Lifton, Richard P, McNiff, Jennifer M, Lucky, Anne W, Choate, Keith A

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